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RAN BIOLINKS DIAGNOSTICS

GENETIC TESTING

Which Genetic Test Is Right For You ?

We offer cutting-edge genetic testing services powered by Next Generation Sequencing (NGS). Harnessing the latest advancements in genomics technology, we offer comprehensive analyses for a wide array of diseases and pathologies. Our NGS-based approach allows for rapid, accurate, and high-throughput sequencing of genetic material, enabling us to provide detailed insights into your genetic makeup with unparalleled precision. By choosing RAN BIOLINKS, you're selecting a trusted partner committed to delivering actionable information that can guide personalized healthcare decisions. Whether you're seeking to understand inherited conditions, assess disease risk, or optimize treatment strategies, our expertise in NGS ensures that you receive the most reliable and informative genetic testing available. Join us on the forefront of genetic innovation and embark on a journey towards a healthier, more informed future.

WHEN COULD YOU ORDER A TEST ?

Family Planning

Couples may undergo genetic testing to assess the risk of passing on hereditary conditions to their children, allowing them to make informed decisions about family planning.

Inherited Diseases

Individuals with a family history of inherited disorders such as cystic fibrosis, Huntington's disease, or sickle cell anemia may opt for genetic testing to determine their risk of developing or passing on these conditions

Cancer Risk Assessment

Those with a family history of certain cancers, such as breast, ovarian, or colorectal cancer, may undergo genetic testing to assess their predisposition to these diseases and to inform early detection and prevention strategies

Pharmacogenomics

Genetic testing can help healthcare providers tailor medication choices and dosages based on an individual's genetic makeup, optimizing treatment efficacy while minimizing adverse drug reactions

Rare Diseases

For individuals experiencing unexplained symptoms or rare medical conditions, genetic testing can aid in identifying underlying genetic mutations responsible for their health issues, leading to more accurate diagnoses and targeted treatment plans

Carrier Screening

Prospective parents may undergo carrier screening to determine if they carry genetic mutations associated with conditions like cystic fibrosis, thalassemia, or Tay-Sachs disease, allowing them to assess the risk of passing these conditions to their offspring

Preventive Health

Some individuals may choose genetic testing to gain insights into their predisposition to certain health conditions, empowering them to adopt lifestyle modifications and preventive measures to mitigate disease risk.

Ancestry & Genealogy

Genetic testing can be used to explore one's ancestry and genetic heritage, providing insights into ethnic origins, migration patterns, and genetic relationships with distant relatives.

HOW TO ORDER A TEST ?

Consult your physician to determine the most suitable test for yourself or a family member.

1

Obtain a sample at the blood drawing point nearest to you.

2

Anticipate receiving the genetic report within 15 to 25 business days.

3

Discuss the results and subsequent steps with your physician.

4

Engage with RAN BioLinks Genetics counselors for assistance in elucidating the results.

5

OUR METHODOLOGY

Our Genomics Pipeline: An Automated Process from Sequencing to Insights

Whole Exome Sequencing (WES) Capabilities

We offer bioinformatics-driven Next Generation Sequencing (NGS) analysis service for whole exome sequencing (WES). Our process begins with precise extraction of genetic material, followed by library preparation and sequencing using cutting-edge NGS technology. Harnessing advanced bioinformatics algorithms, we meticulously analyze the exonic regions of your genome, identifying genetic variants with clinical significance. From variant calling to comprehensive annotation and interpretation, we deliver actionable insights into inherited conditions, disease risk, and pharmacogenomic traits, empowering informed healthcare decisions tailored to your unique genetic profile.

Whole Genome Sequencing (WGS) Capabilities

We offer genomic discovery with our whole genome sequencing (WGS) analysis service. Our process starts with the extraction of genetic material, followed by library preparation and sequencing using state-of-the-art NGS technology. Leveraging advanced bioinformatics algorithms, we comprehensively analyze your entire genome, identifying genetic variants with clinical relevance. Through precise variant calling, thorough annotation, and insightful interpretation, we provide a holistic view of your genetic makeup, offering valuable insights into disease predisposition, inherited conditions, and pharmacogenomic traits. Trust in our expertise to deliver accurate and actionable results, guiding personalized healthcare strategies based on your individual genetic landscape

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Location : 
10212 Yonge Street, 202, Richmond Hill, Ontario, Canada, L4C 3B6

Email : 
[email protected]

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